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1
المؤلفون: L. Tranebjaerg, Richard J.H. Smith, M. Z. Pelias, J. F. Hejtmancik, Bronya J.B. Keats, Richard A. Lewis, Claes Möller, Charles I. Berlin, William J. Kimberling
المصدر: American Journal of Medical Genetics. 50:32-38
مصطلحات موضوعية: Pediatrics, medicine.medical_specialty, business.industry, MYO7A, Usher syndrome, Usher Syndrome Type 1, medicine.disease, eye diseases, Clinical diagnosis, otorhinolaryngologic diseases, Medicine, business, Genetics (clinical), PCDH15
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2
المؤلفون: Elizabeth C. Lee, J. Fielding Hejtmancik, Stephen P. Daiger, Mary Guest, Alan C. Bird, Bronya J.B. Keats, William Reardon, William J. Kimberling, Richard J.H. Smith, M. Z. Pelias, Radha Ayyagari, Marcelle Jay
المصدر: Genomics. 14:995-1002
مصطلحات موضوعية: Male, Genetic Linkage, MYO7A, Usher syndrome, Population, Biology, Locus heterogeneity, Genetic linkage, otorhinolaryngologic diseases, Genetics, medicine, Humans, education, Hearing Disorders, education.field_of_study, Polymorphism, Genetic, Genetic heterogeneity, Chromosomes, Human, Pair 11, Usher Syndrome Type 1, Chromosome Mapping, Chromosome, Syndrome, medicine.disease, Pedigree, Female, Lod Score, Retinitis Pigmentosa
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3
المؤلفون: Richard A. Lewis, William J. Kimberling, Mark Leppert, J. Fielding Hejtmancik, Alexander A. Todorov, Richard J.H. Smith, M. Z. Pelias, Bronya J.B. Keats, Larry D. Atwood
المصدر: Genomics. 14:707-714
مصطلحات موضوعية: Genetic Markers, Genetics, Genetic Linkage, Hearing loss, Usher syndrome, Usher Syndrome Type 1, Chromosome Mapping, Genes, Recessive, Locus (genetics), Syndrome, Deafness, Biology, medicine.disease, eye diseases, Gene mapping, Genetic linkage, Genetic marker, Retinitis pigmentosa, otorhinolaryngologic diseases, medicine, Chromosomes, Human, Humans, medicine.symptom, Retinitis Pigmentosa
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4
المؤلفون: J. F. Hejtmancik, Stephen P. Daiger, Bronya J.B. Keats, William J. Kimberling, Richard J.H. Smith, M. Z. Pelias
المصدر: American Journal of Medical Genetics. 43:964-969
مصطلحات موضوعية: Genetic Markers, Male, Hearing loss, Usher syndrome, Population, Ethnic group, Biology, Blindness, Genotype, Ethnicity, medicine, Humans, education, Hearing Disorders, Genetics (clinical), Psychomotor learning, education.field_of_study, Genetic heterogeneity, fungi, Syndrome, Louisiana, medicine.disease, Phenotype, Pedigree, Chromosomes, Human, Pair 1, Evolutionary biology, Female, medicine.symptom
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5
المؤلفون: M Z, Pelias, M M, DeAngelis
المصدر: Loyola law review. 45(2)
مصطلحات موضوعية: Cryopreservation, Genetics, Medical, Wrongful Life, Genetic Diseases, Inborn, Legislation as Topic, Genetic Counseling, Genetic Therapy, Embryo, Mammalian, Gamete Intrafallopian Transfer, Prenatal Diagnosis, Adoption, Humans, Female, Embryo Disposition, Genetic Testing, Genetic Privacy, Preimplantation Diagnosis
URL الوصول: https://explore.openaire.eu/search/publication?articleId=pmid________::e6e893da3894729143d234f196c99fa2
https://pubmed.ncbi.nlm.nih.gov/16622958 -
6
المؤلفون: M Z, Pelias, N J, Markward
المصدر: Emory law journal. 49(3)
مصطلحات موضوعية: Patents as Topic, Genetic Research, Informed Consent, Eugenics, Genetics, Medical, Human Genome Project, Humans, Genetic Counseling, Genetic Testing, Genetic Privacy, Confidentiality
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7
المؤلفون: R, Ayyagari, Y, Li, R J, Smith, M Z, Pelias, J F, Hejtmancik
المصدر: Molecular vision. 1
مصطلحات موضوعية: Canada, Haplotypes, Chromosomes, Human, Pair 11, Hearing Loss, Sensorineural, Chromosome Mapping, Humans, France, Syndrome, Louisiana, Retinitis Pigmentosa, Microsatellite Repeats
URL الوصول: https://explore.openaire.eu/search/publication?articleId=pmid________::82d300f8cf30ff26a37c8160b91711a6
https://pubmed.ncbi.nlm.nih.gov/9238080 -
8
المؤلفون: B J, Keats, N, Nouri, M Z, Pelias, P L, Deininger, M, Litt
المصدر: American journal of human genetics. 54(4)
مصطلحات موضوعية: Genetic Markers, Genetic Linkage, Chromosomes, Human, Pair 11, Quebec, Syndrome, DNA, Satellite, Deafness, Louisiana, Pedigree, Genetics, Population, Haplotypes, otorhinolaryngologic diseases, Humans, Lod Score, Retinitis Pigmentosa, Research Article
URL الوصول: https://explore.openaire.eu/search/publication?articleId=pmid________::5e92e1f451b52c112a673d59092e1ad7
https://pubmed.ncbi.nlm.nih.gov/8128966 -
9
المؤلفون: R J, Smith, C I, Berlin, J F, Hejtmancik, B J, Keats, W J, Kimberling, R A, Lewis, C G, Möller, M Z, Pelias, L, Tranebjaerg
المصدر: American journal of medical genetics. 50(1)
مصطلحات موضوعية: Diagnosis, Differential, Ophthalmoscopy, Vestibular Diseases, Hearing Loss, Sensorineural, Surveys and Questionnaires, Electroretinography, Humans, Syndrome, Vestibular Function Tests, Retinitis Pigmentosa
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10
المؤلفون: H A, Lubs, L J, Elsas, A T, Tharapel, P D, Buchanan, W H, Finley, C B, Lozzio, M Z, Pelias
المصدر: American journal of medical genetics. 46(4)
مصطلحات موضوعية: Pregnancy, Prenatal Diagnosis, Humans, Female, Interphase, In Situ Hybridization